Using myMedidata in Your Clinical Trials eLearning Modules

Overview

Below covers all the training courses available for myMedidata functionality. The courses will provide you with an introduction on the suite of myMedidata products that can be used in any type of study (Onsite, Remote, Hybrid).

Instead of being assigned to a course with several modules as a standard, clients will assign the modules from the list below based on each sponsor's unique needs.

Note: Clients are not required to select all modules. They will select only the modules that reflect their study setup.

Getting Started: Using myMedidata in Your Clinical Trial  

Prerequisite

20 mins

This course is intended for Site Users and Administrators and provides a thorough understanding of how to support or manage myMedidata studies to carry out common tasks and responsibilities. For example, you will learn how:

• To invite Patients to a myMedidata Study
• Patients Create a myMedidata Account
• To manage Patients in the Patient Management Dashboard

Using myMedidata eCOA in Your Clinical Trial

Optional

7 mins

This course is intended for Site Users and Administrators and provides a thorough understanding of how to support or manage myMedidata studies to carry out common tasks and responsibilities. For example, you will learn how:

• Patients Access eCOA Forms in myMedidata eCOA
• Patients Complete and Submit eCOA Forms from their myMedidata Account

Using myMedidata LIVE in Your Clinical Trial

Optional

18 mins

This course is intended for Site Users and Administrators and provides a thorough understanding of how to support or manage myMedidata studies to carry out common tasks and responsibilities. For example, you will learn how:

• To invite Patients to a Video Visit
• To Bypass a Video Visit
• Patients and Supporting Participants Launch a Scheduled Video Visit
• Patients and Supporting Participants Request, Reschedule, or Cancel a Video Visit

Using myMedidata eConsent in Your Clinical Trial

Optional

15 mins

This course is intended for Site Users and Administrators and provides a thorough understanding of how to support or manage myMedidata studies to carry out common tasks and responsibilities. For example, you will learn how:

• Patients Consent with myMedidata eConsent
• Patients Consent when a Video Visit is Required
• Patients Consent with No Video Visit
• Patients Sign the Informed Consent Form (ICF)
• Clinicians Countersign the Informed Consent Form (ICF)

Using Rave RTSM in You myMedidata Clinical Trial

Optional

6 mins

This course is intended for Site Users and Administrators and provides a thorough understanding of how to support or manage myMedidata studies to carry out common tasks and responsibilities. For example, you will learn how:

• Patients Track their Shipments in their myMedidata Account
• Patients can Mark their Shipment as Received With or Without any Issues To Notify If a Shipment has been Received or Not

Using myMedidata Registries in Your Clinical Trial

Optional

20 mins

This course is intended for Site Users and Administrators and provides a thorough understanding of how to support or manage myMedidata studies to carry out common tasks and responsibilities. For example, you will learn how:

• New and Existing Participants Enroll into a myMedidata Registry
• Clinicians Review and Determine Participants Eligibility to a Registry
• Clinicians Invite a Participant from a Registry to a Study
• Clinicians Invite a Participant from a Study to a Registry

Recording of Global Education training sessions is strictly prohibited. Any attempts to record training will result in an immediate stoppage of training until recording is terminated.